Discover practical AI expertise for medical devices!
Artificial intelligence is transforming medical technology – yet regulatory requirements are increasing significantly. This is exactly where our hands-on training “Artificial Intelligence (AI) in Medical Devices” comes in: a compact, highly practice‑oriented online workshop that guides you safely through standards, processes, and new legal obligations.
Our expertise – made practical for you!
Regulatory excellence – step by step:
Learn how to develop and document AI models in compliance with the MDR, IVDR and the new EU Artificial Intelligence Act (AIA) – a crucial factor for the successful market approval of AI‑based medical devices.
Training based on a real example:
You will work with a real, publicly available AI model with a medical purpose and learn to apply AIA‑ and MDR‑compliant templates efficiently. You will later receive these documents as a PDF – including a complete list of requirements for high-risk AI medical devices.
Ideal for regulatory and quality management teams:
The training is aimed at professionals in MedTech companies who are responsible for regulatory compliance of AI‑based products. No programming skills are required – the focus is on practical implementation.
What to expect in the workshop
- Introduction to a fictional MedTech company and its AI software
- Training & testing of a simple neural network – limited to what is relevant for regulatory requirements
- Step-by-step application of current AIA/MDR templates
- Transfer of learnings to your own products
- Practice-oriented discussions with subject-matter experts
Your Trainer
Dr Thorsten Prinz (VDE, Offenbach/Main) – Expert in digital transformation and AI regulation. > LinkedIn
Secure your place now!
Bring your expertise up to date and prepare your company for the future of AI‑powered medical technology.
